A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950209



Internal ID17299083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:45184202..45191301hg38UCSC Ensembl
Outerchr7:45223801..45230900hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997644
SamplesBILGI_BIOE
Known GenesRAMP3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950209
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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